Association of TP53 codon 72 polymorphism and the outcome of adjuvant therapy in breast cancer patients

被引:83
作者
Toyama, Tatsuya
Zhang, Zhenhuan
Nishio, Mariko
Hamaguchi, Maho
Kondo, Naoto
Iwase, Hirotaka
Iwata, Hiroji
Takahashi, Satoru
Yamashita, Hiroko
Fujii, Yoshitaka
机构
[1] Nagoya City Univ, Grad Sch Med Sci, Dept Oncol Immunol & Surg, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[2] Kumamoto Univ, Grad Sch Med Sci, Dept Breast & Endocrine Surg, Kumamoto 8608556, Japan
[3] Aichi Canc Ctr Hosp, Dept Breast Oncol, Chikusa Ku, Nagoya, Aichi 4648681, Japan
[4] Nagoya City Univ, Grad Sch Med Sci, Dept Expt Pathol & Tumor Biol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
[5] Nagoya City Univ Hosp, Div Pathol, Mizuho Ku, Nagoya, Aichi 4678601, Japan
关键词
D O I
10.1186/bcr1682
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Single-nucleotide polymorphisms ( SNPs) in codon 72 of the TP53 ( also known as p53) gene ( rs1042522) and in the promoter region of the MDM2 gene ( SNP309; rs2279744) have been suggested to play roles in many cancers. We investigated whether these SNPs were associated with patient outcome and the effect of adjuvant systemic therapy. Methods The genotypes of TP53 codon 72 and MDM2 SNP309 were defined among 557 primary Japanese breast cancer patients ( median follow-up, 61.7 months). The effects of several variables on survival were tested by Cox's proportional hazards regression analysis. Results We showed that the Pro/Pro genotype of TP53 codon 72 was associated with poorer disease-free survival ( DFS) than other genotypes by Kaplan-Meier analysis ( P = 0.049) and multivariate Cox's proportional hazards regression analysis ( P = 0.047, risk ratio of recurrence = 1.67), whereas MDM2 SNP309 status was not associated with DFS. The association of the Pro/Pro TP53 genotype with poorer DFS was especially significant in patients who received adjuvant chemotherapy ( P = 0.009). In contrast, among the patients who had received adjuvant hormonal therapy or no adjuvant systemic therapy, TP53 codon 72 genotype was not associated with DFS. Conclusion The Pro/Pro genotype of TP53 codon 72 appears to be an independent prognostic marker in breast cancer patients.
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页数:10
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共 46 条
[1]   A chromatin-associated and transcriptionally inactive p53-Mdm2 complex occurs in mdm2 SNP309 homozygous cells [J].
Arva, NC ;
Gopen, TR ;
Talbott, KE ;
Campbell, LE ;
Chicas, A ;
White, DE ;
Bond, GL ;
Levine, AJ ;
Bargonetti, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (29) :26776-26787
[2]   Immunohistochemical status of p53, MDM2, bcl2, bax, and ER in invasive ductal breast carcinoma in Tunisian patients [J].
Baccouche, S ;
Daoud, J ;
Frikha, M ;
Mokdad-Gargouri, R ;
Gargouri, A ;
Jlidi, R .
APOPTOSIS: FROM SIGNALING PATHWAYS TO THERAPEUTIC TOOLS, 2003, 1010 :752-763
[3]  
Barbareschi M, 1996, APPL IMMUNOHISTOCHEM, V4, P106
[4]   Association of breast cancer outcome with status of p53 and MDM2 SNP309 [J].
Boersma, Brenda J. ;
Howe, Tiffany M. ;
Goodman, Julie E. ;
Yfantis, Harry G. ;
Lee, Dong H. ;
Chanock, Stephen J. ;
Ambs, Stefan .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2006, 98 (13) :911-919
[5]  
Bonafé M, 2003, CLIN CANCER RES, V9, P4860
[6]   MDM2 SNP309 accelerates tumor formation in a gender-specific and hormone-dependent manner [J].
Bond, Gareth L. ;
Hirshfield, Kim M. ;
Kirchhoff, Tomas ;
Alexe, Gabriella ;
Bond, Elisabeth E. ;
Robins, Harlan ;
Bartel, Frank ;
Taubert, Helge ;
Wuerl, Peter ;
Hait, William ;
Toppmeyer, Deborah ;
Offit, Kenneth ;
Levine, Arnold J. .
CANCER RESEARCH, 2006, 66 (10) :5104-5110
[7]   A single nucleotide polymorphism in the MDM2 promoter attenuates the p53 tumor suppressor pathway and accelerates tumor formation in humans [J].
Bond, GL ;
Hu, WW ;
Bond, EE ;
Robins, H ;
Lutzker, SG ;
Arva, NC ;
Bargonetti, J ;
Bartel, F ;
Taubert, H ;
Wuerl, P ;
Onel, K ;
Yip, L ;
Hwang, SJ ;
Strong, LC ;
Lozano, G ;
Levine, AJ .
CELL, 2004, 119 (05) :591-602
[8]  
BUESORAMOS CE, 1996, BREAST CANC RES TREA, V37, P197
[9]   Robustness, scalability, and integration of a wound-response gene expression signature in predicting breast cancer survival [J].
Chang, HY ;
Nuyten, DSA ;
Sneddon, JB ;
Hastie, T ;
Tibshirani, R ;
Sorlie, T ;
Dai, HY ;
He, YDD ;
van't Veer, LJ ;
Bartelink, H ;
van de Rijn, M ;
Brown, PO ;
van de Vijver, MJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (10) :3738-3743
[10]  
CORDONCARDO C, 1994, CANCER RES, V54, P794